Andersen-Tawil syndrome

Disease Export to PDF
Name:
Andersen-Tawil syndrome
Description:
A rare disorder characterized by periodic muscle paralysis, prolongation of the QT interval with a variety of ventricular arrhythmias (leading to predisposition to sudden cardiac death) and characteristic physical features: short stature, scoliosis, low-set ears, hypertelorism, broad nasal root, micrognathia, clinodactyly, brachydactyly and syndactyly.
ORPHAcode:
37553
Synonyms:
Andersen syndrome
LQT7
Long QT syndrome type 7
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14